Variant #0000574862 (NC_000023.10:g.153648452_153648453insG, TAZ(NM_000116.3):c.646+19_646+20insG)

Chromosome X
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.153648452_153648453insG
DNA change (hg38) g.154420113_154420114insG
Published as -
ISCN -
DB-ID DNASE1L1_000034
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Variant not found in online data sets
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TAZ NM_000116.3 -?/. - c.646+19_646+20insG r.(=) p.(=)
DNASE1L1 NM_001009932.1 -?/. - c.-8656_-8655insC r.(?) p.(=)